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A special gene region controls the re-emergence of a primitive wool type in Merino sheep, improving their wool yield and adaptability.

The research mapped gene activity in developing mouse skin and found key markers for skin cell types and changes from fetal to early postnatal stages.

Deleting the Hoxc13 gene in frogs shows its crucial role in developing skin structures similar to hair.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Deleting the CD271 gene in mouse skin cells leads to disorganized skin and increased hair growth, suggesting CD271 is important for skin health.

Certain ESR1 gene variations may affect hormone levels and fat distribution in women with high male hormone levels.

Turning off the Lhx2 gene in mouse embryos leads to slower wound healing and scars.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

Disrupting the Tsc2 gene in certain cells leads to thicker skin, larger hair, and changes in hair growth signaling, which can be partly reversed with specific treatment.

Mutations in the FOXN1 gene cause severe immune issues but don't affect hair and nails.

Patients with certain FoxN1 gene mutations have severe immune issues but normal skin and hair.

Removing the Crif1 gene in mouse skin disrupts skin balance and hair growth.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

New treatments for hair growth and psoriasis may be possible, and gene differences could affect baldness and the severity of skin conditions.

Balding scalps show different gene expressions affecting hair growth compared to non-balding scalps.

The Engrailed-1 gene plays a key role in the development of sweat glands in mice.

A certain gene variation can affect protein production and is linked to male pattern baldness.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

Methylation in specific gene region causes finasteride resistance in some BPH patients.

The research shows that a gene called Wnt3 affects hair growth and structure, causing short hair and balding when overactive.

Mice lacking the PPARγ gene in their fat cells had almost no fat tissue, severe metabolic problems, and abnormal development of other fat-related tissues.

Planarian regeneration begins with a specific gene activation caused by injury, essential for healing and tissue regrowth.

A genetic region near the PAX1 gene is linked to a higher risk of scoliosis in females.

The article concludes that better understanding gene regulation related to seasonal changes can offer insights into the mechanisms of seasonal timing in mammals.

Certain mutations in the H6PD gene cause Cortisone Reductase Deficiency by affecting hormone production.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Hair growth is controlled by specific gene clusters and proteins, and cysteine affects hair gene expression in sheep.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.